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Occult Nesidioblastosis Detected by 111In-Pentetreotide Single-Photon Emission Computed Tomography. 通过 111In-Pentetreotide 单光子发射计算机断层扫描发现的隐匿性网状母细胞增生症
IF 0.6 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2024-10-01 DOI: 10.18926/AMO/67667
Shinya Sakamoto, Motoyasu Tabuchi, Rika Yoshimatsu, Ai Hishida, Manabu Matsumoto, Jun Iwata, Takehiro Okabayashi

Nesidioblastosis, also known as persistent hyperinsulinemic hypoglycemia, is usually observed in children and infants, although more recently adult-onset nesidioblastosis has also been described. We present a case of nesidioblastosis in a 78-year-old man that was detected by 111In-pentetreotide single photon emission computed tomography (SPECT/CT). The patient was transferred to our hospital's emergency department in a hypoglycemic coma. Dynamic enhanced CT could detect no lesion in the pancreas, but an 111In-pentetreotide SPECT/CT scan performed after a similar episode four weeks later showed increased focal uptake at the head of the pancreas. The results of a selective arterial calcium injection test were negative. After careful consideration and discussion among colleagues, surgical intervention was selected, and a pancreaticoduodenectomy was performed. On histology, there were elevated numbers of Langerhans islets in the pancreatic head, and the islets themselves appeared enlarged. Hypertrophic β-cells comprised the majority, but α-cells, δ-cells and pancreatic polypeptide were also detected in the islets. Based on the histopathological results and repeated hyperinsulinemic hypoglycemic crises, the patient was finally diagnosed with adult-onset nesidioblastosis. He had no hypoglycemic symptoms during outpatient follow-up examination. Since 111In-pentetreotide SPECT/CT may be able to detect nesidioblastosis, clinicians should consider this relatively new-modality examination when encountering such cases.

内异胰岛素母细胞增多症又称持续性高胰岛素血症性低血糖,通常发生在儿童和婴儿身上,但最近也有成人发病的内异胰岛素母细胞增多症。我们介绍了一例通过 111In- 五孕肽单光子发射计算机断层扫描(SPECT/CT)检测出的 78 岁男性非胰岛素母细胞增多症。患者在低血糖昏迷状态下被转到我院急诊科。动态增强 CT 未发现胰腺病变,但在四周后的一次类似病发后进行的 111In-pentetreotide SPECT/CT 扫描显示,胰腺头部的灶性摄取增加。选择性动脉钙注射试验结果为阴性。经过慎重考虑和同事讨论后,患者选择了手术治疗,并进行了胰十二指肠切除术。组织学检查显示,胰腺头部的朗格汉斯小体数量增加,小体本身也增大。肥大的β细胞占多数,但也能在小球中检测到α细胞、δ细胞和胰多肽。根据组织病理学结果和反复出现的高胰岛素低血糖危象,患者最终被诊断为成人型无胰岛细胞病。在门诊随访检查中,他没有出现低血糖症状。由于111In-戊四肽酶SPECT/CT可检测出内胚叶增生症,临床医生在遇到此类病例时应考虑采用这种相对较新的检查方式。
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引用次数: 0
The First Report of Bickerstaff Brainstem Encephalitis Induced by Atezolizumab for Metastatic Breast Cancer. 阿特珠单抗治疗转移性乳腺癌诱发比克斯塔夫脑干脑炎的首次报道
IF 0.6 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2024-10-01 DOI: 10.18926/AMO/67665
Kyoko Shimoyama, Atsushi Nakajima, Yoshimitsu Minari

Immune checkpoint inhibitors (ICIs) have revolutionized cancer treatment, but they have been known to cause immune-related adverse events (irAEs) by promoting T-cell activation. Neurological irAEs are rare (1%) but have a high fatality rate (11.5%). Here we report the first case of Bickerstaff brainstem encephalitis (BBE) induced by an ICI. A woman in her 60s with metastatic breast cancer was treated with atezolizumab plus nab-paclitaxel once intravenously. Eighteen days later, she lost consciousness with ophthalmoplegia and was diagnosed with a neurological irAE. She recovered consciousness immediately with the administration of intravenous immunoglobulin (IVIG) but suffered severe permanent peripheral neuropathy. Although it is just one case, this experience shows that BBE occurring as a neurological irAE of ICI cancer treatment may be associated with more severe outcomes than conventional BBE in metastatic cancer. Creating a system for multidisciplinary treatment is essential for ICI therapy.

免疫检查点抑制剂(ICIs)给癌症治疗带来了革命性的变化,但已知它们会通过促进T细胞活化而导致免疫相关不良事件(irAEs)。神经系统的irAEs非常罕见(1%),但致死率却很高(11.5%)。在此,我们报告了首例由 ICI 诱发的 Bickerstaff 脑干脑炎(BBE)病例。一名 60 多岁的转移性乳腺癌患者接受了阿特珠单抗加纳布紫杉醇静脉注射一次的治疗。18 天后,她因眼球震颤而失去知觉,被诊断为神经系统虹膜AE。通过静脉注射免疫球蛋白(IVIG),她立即恢复了意识,但却遭受了严重的永久性周围神经病变。虽然这只是一个病例,但这一经历表明,在 ICI 癌症治疗过程中出现的神经系统损伤性脑血管病可能会比传统的转移性脑血管病带来更严重的后果。建立多学科治疗系统对于 ICI 治疗至关重要。
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引用次数: 0
Phenotypic and Genetic Characteristics of Carbapenemase-Producing Enterobacterales Isolates at Okayama University Hospital. 冈山大学医院产碳青霉烯酶肠杆菌属分离菌的表型和遗传特征。
IF 0.6 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2024-10-01 DOI: 10.18926/AMO/67657
Kazuyoshi Gotoh, Makoto Miyoshi, I Putu Bayu Mayura, Shuma Tsuji, Koji Iio, Shinnosuke Fukushima, Osamu Matsushita, Hideharu Hagiya

Spread of carbapenemase-producing Enterobacterales (CPE) is an ongoing public health issue worldwide, including in Japan. In this study, we investigated the phenotypic and genetic characteristics of CPE isolates at Okayama University Hospital over the 5 years (2013-2018) prior to the outbreak of the 2019 coronavirus pandemic. Of 24 carbapenem-resistant Enterobacterales isolated during the study period, we identified 8 CPE isolates harboring blaIMP-1 (5 isolates) and blaIMP-6 genes (3 isolates). Bacterial species and carbapenem susceptibility patterns exhibited diversity. Minimum inhibitory concentrations (MICs) of meropenem were generally higher than those of imipenem and biapenem. Results of pulsed-field gel electrophoresis demonstrated that neither clonal nor plasmid-mediated outbreaks of blaIMP-harboring CPE isolates have developed at our hospital. One Klebsiella oxytoca isolate showed a high MIC (128 μg/mL) of meropenem, which could be explained by the high plasmid copy number. Subsequent analysis of this isolate may elucidate the intricacies of carbapenem resistance profiles among CPE isolates. Collectively, our findings underscore the necessity for ongoing genetic surveillance of CPE, complemented by tailored approaches for infection prevention and control.

产碳青霉烯酶肠杆菌(CPE)的传播是包括日本在内的全球持续存在的公共卫生问题。在本研究中,我们调查了冈山大学医院在 2019 年冠状病毒大流行爆发前 5 年(2013-2018 年)分离到的 CPE 的表型和遗传特征。在研究期间分离的 24 个耐碳青霉烯类肠杆菌中,我们发现 8 个 CPE 分离物携带 blaIMP-1 基因(5 个分离物)和 blaIMP-6 基因(3 个分离物)。细菌种类和碳青霉烯类药物敏感性模式呈现出多样性。美罗培南的最低抑菌浓度(MICs)普遍高于亚胺培南和比亚培南。脉冲场凝胶电泳结果表明,本医院既没有出现由克隆或质粒介导的携带 blaIMP 的 CPE 分离物爆发。其中一个氧合克雷伯氏菌分离物对美罗培南的 MIC 值很高(128 μg/mL),这可能与质粒拷贝数较高有关。对该分离株的后续分析可能会阐明 CPE 分离株对碳青霉烯类耐药性的复杂性。总之,我们的研究结果表明,有必要对 CPE 进行持续的基因监测,并辅以有针对性的感染预防和控制方法。
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引用次数: 0
Focal Cerebral Hypoperfusion Detected by Arterial Spin-Labeled Magnetic Resonance Imaging in Patients with Migraine Presenting with Neurological Symptoms Concomitant with or without Headache. 通过动脉自旋标记磁共振成像检测伴有或不伴有头痛的偏头痛患者的神经症状的局部脑灌注不足。
IF 0.6 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2024-10-01 DOI: 10.18926/AMO/67666
Kenichi Kashihara, Minoru Irisawa, Wataru Takao

We investigated patients with migraine or migraine variants who exhibited focal cerebral hypoperfusion on arterial spin-labeled (ASL) magnetic resonance (MR) imaging along with neurological symptoms. Fourteen patients with migraine demonstrated focal cerebral hypoperfusion. Three other patients did not have a history of recurrent headaches but exhibited comparable cerebral hypoperfusion to migraine patients on ASL-MRI in addition to neurological symptoms. Patients with migraine may present with neurological symptoms associated with cortical spreading depression during, after, or even without a headache phase. Additionally, the isolated neurological symptoms may be caused by a pathophysiology identical to that of migraine but without presenting with recurrent headaches.

我们对动脉自旋标记(ASL)磁共振(MR)成像显示局灶性脑灌注不足并伴有神经症状的偏头痛或偏头痛变异型患者进行了调查。14 名偏头痛患者表现出局灶性脑灌注不足。另有三名患者没有复发性头痛病史,但在 ASL-MRI 上表现出与偏头痛患者相似的脑灌注不足,同时伴有神经系统症状。偏头痛患者可能会在头痛期、头痛期之后甚至没有头痛期的情况下出现与皮质扩散抑制相关的神经症状。此外,孤立的神经症状可能是由与偏头痛相同的病理生理学引起的,但并不表现为复发性头痛。
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引用次数: 0
Pediatric Severe Febrile Thrombocytopenia Syndrome: A Case Report and Literature Review. 小儿严重发热性血小板减少综合征:病例报告和文献综述。
IF 0.6 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2024-10-01 DOI: 10.18926/AMO/67664
Yusuke Toyota, Kazuhiro Uda, Komei Shirabe, Tadashi Moriwake

Severe febrile thrombocytopenia syndrome (SFTS) is a tick-borne infectious disease that is endemic in parts of eastern Asia. Few pediatric cases have been reported. We describe a case of SFTS in a seven-year-old girl who presented with prolonged fever and gastrointestinal symptoms. Leukopenia and thrombocytopenia on hematology, and a history of outdoor activity led us to diagnose SFTS, although the patient had no tick bite marks. We also review the literature and discuss the characteristics of pediatric SFTS. Physicians should consider SFTS in the differential diagnosis of fever with thrombocytopenia in children living in endemic areas.

严重发热血小板减少综合征(SFTS)是一种蜱媒传染病,在亚洲东部部分地区流行。儿科病例鲜有报道。我们描述了一例七岁女孩的严重发热性血小板减少综合征病例,该女孩表现为长期发热和胃肠道症状。虽然患者身上没有蜱虫叮咬的痕迹,但血液学检查结果显示白细胞和血小板减少,而且患者有户外活动史,因此我们诊断其为自发性蜱虫病。我们还回顾了相关文献,并讨论了小儿 SFTS 的特征。医生在鉴别诊断生活在地方病流行地区的发热伴血小板减少的儿童时应考虑 SFTS。
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引用次数: 0
Factors Affecting Dynamic Postural Control Ability in Adolescent Idiopathic Scoliosis. 影响青少年特发性脊柱侧凸动态姿势控制能力的因素。
IF 0.6 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2024-10-01 DOI: 10.18926/AMO/67655
Ryoko Yamawaki, Yoshiaki Oda, Shuhei Yamane, Koji Uotani, Haruo Misawa, Yoshimi Katayama, Masanori Hamada, Toshifumi Ozaki

Research on postural control in patients with adolescent idiopathic scoliosis (AIS) has focused on static postural control, with few studies assessing dynamic postural control. We aimed to identify factors affecting index of postural stability (IPS), a dynamic postural control parameter, in patients with AIS. The participants comprised 50 female patients with AIS. We measured the IPS using stabilometry to evaluate dynamic postural control ability. We investigated age of the participants, major curve position (thoracic or thoracolumbar/lumbar), Cobb angle, and coronal balance. We then assessed the relationships between stabilometry parameters and other variables. IPS was analyzed with a linear regression model. Coronal balance, major curve position, and age each correlated with dynamic postural control ability. The Cobb angle showed no correlation with any of the parameters. Our results offer new insights into the assessment of postural control in patients with AIS.

有关青少年特发性脊柱侧弯症(AIS)患者姿势控制的研究主要集中在静态姿势控制方面,很少有研究对动态姿势控制进行评估。我们旨在确定影响 AIS 患者动态姿势控制参数--姿势稳定性指数(IPS)的因素。研究对象包括 50 名女性 AIS 患者。我们使用稳定测量法测量了 IPS,以评估动态姿势控制能力。我们调查了参与者的年龄、主要曲线位置(胸椎或胸腰椎/腰椎)、Cobb 角和冠状平衡。然后,我们评估了稳定测量参数与其他变量之间的关系。IPS 采用线性回归模型进行分析。冠状平衡、主要曲线位置和年龄均与动态姿势控制能力相关。Cobb 角与任何参数均无相关性。我们的研究结果为评估 AIS 患者的姿势控制能力提供了新的视角。
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引用次数: 0
Small-for-Gestational-Age Status and the Risk of Kawasaki Disease: A Nationwide Birth Cohort in Japan. 小于胎龄状态与川崎病风险:日本全国出生队列。
IF 0.6 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2024-10-01 DOI: 10.18926/AMO/67656
Satoe Takanaga, Naomi Matsumoto, Tomoka Kadowaki, Soshi Takao, Takashi Yorifuji

Kawasaki disease (KD) is a pediatric disease of unknown etiology that commonly affects infants in East Asia. Infants born small for gestational age (SGA) have weaker immune systems and are more susceptible to infection. Using data from a nationwide Japanese birth cohort study conducted in 2010 (n=34,579), we investigated whether SGA increases the risk of KD. SGA was defined as birth weight below the 10th percentile for gestational age. The outcome was hospitalization for KD between 6 and 30 months of age. The association between SGA and hospitalization for KD, adjusted for child and maternal factors, was examined using logistic regression. Of the 231 children hospitalized for KD, 9.5% were SGA. Further statistical analysis showed that SGA did not increase the odds ratio (OR) of hospitalization for KD (adjusted OR 1.12, 95% confidence interval 0.71-1.75). This result was not changed with stratification by early daycare attendance and preterm status. Reasons for the lack of association may include the multifactorial pathogenesis of KD; in addition, the types of infections to which SGA infants are predisposed may differ from those triggering KD. Overall, our large nationwide study found no association between SGA and KD.

川崎病(Kawasaki disease,KD)是一种病因不明的儿科疾病,常见于东亚地区的婴儿。胎龄小的婴儿(SGA)免疫系统较弱,更容易受到感染。我们利用 2010 年进行的一项日本全国性出生队列研究的数据(n=34,579),研究了 SGA 是否会增加 KD 的风险。SGA 的定义是出生体重低于胎龄第 10 百分位数。研究结果显示,6 到 30 个月大的婴儿因 KD 而住院。在对儿童和母体因素进行调整后,采用逻辑回归法检验了 SGA 与 KD 住院之间的关系。在 231 名因 KD 住院的儿童中,9.5% 患有 SGA。进一步的统计分析显示,SGA并不会增加KD住院的几率比(OR)(调整后的OR为1.12,95%置信区间为0.71-1.75)。根据早期入托情况和早产情况进行分层后,这一结果也没有改变。缺乏关联的原因可能包括 KD 的多因素发病机制;此外,SGA 婴儿易受感染的类型可能与引发 KD 的感染类型不同。总之,我们的大型全国性研究发现,SGA 与 KD 之间没有关联。
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引用次数: 0
Can Pelvic Lymph Node Dissection in Prostate Cancer Patients with a 5% Briganti Nomogram Cut-off Value Provide an Oncological Benefit? A Large Multi-Institutional Cohort Study in Japan. 5% Briganti Nomogram 临界值的前列腺癌患者盆腔淋巴结清扫能带来肿瘤学获益吗?日本一项大型多机构队列研究。
IF 0.6 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2024-08-01 DOI: 10.18926/AMO/67546
Naoya Sugihara, Katsuyoshi Hashine, Natsumi Yamashita, Miki Sakamoto, Masato Terashita, Keisuke Funaki, Kaori Saiki, Takatora Sawada, Toshio Kakuda, Kenichi Nishimura, Tetsuya Fukumoto, Noriyosi Miura, Yuki Miyauchi, Tadahiko Kikugawa, Takashi Saika

The Briganti nomogram (cut-off value 5%) is commonly used to determine the indications for pelvic lymph node dissection (PLND) in patients with prostate cancer. We retrospectively analyzed the potential oncological benefit of PLND based on the 5% cut-off value on the Briganti nomogram. We obtained the data from the Medical Investigation Cancer Network (MICAN) Study, which included 3,463 patients who underwent a radical prostatectomy (RP) at nine institutions in Japan between 2010 and 2020. We included patients with Briganti scores ≥ 5% and a follow-up period ≥6 months and excluded patients categorized in the very high-risk group (based on NCCN categories); a final total of the cases of 1,068 patients were analyzed. The biochemical recurrence (BCR)-free survival was significantly worse in the patients who underwent PLND compared to those who did not (p=0.019). A multivariate analysis showed that high prostate-specific antigen (PSA) levels (p<0.001) and an advanced T-stage (p=0.018) were significant prognostic factors for BCR, whereas PLND had no effect on BCR (p=0.059). Thus, PLND in patients with prostate cancer whose Briganti score was 5% did not provide any oncological benefit. Further research is necessary to determine the indication criteria for conducting PLND.

Briganti提名图(临界值为5%)通常用于确定前列腺癌患者盆腔淋巴结清扫(PLND)的适应症。我们根据布里甘蒂提名图的 5%临界值对 PLND 的潜在肿瘤学益处进行了回顾性分析。我们从癌症医学调查网络(MICAN)研究中获得了数据,该研究纳入了2010年至2020年期间在日本九家医疗机构接受根治性前列腺切除术(RP)的3463名患者。我们纳入了布里甘蒂评分≥5%且随访时间≥6个月的患者,并排除了被归类为极高风险组(基于NCCN分类)的患者;最终共分析了1,068例患者。与未接受PLND治疗的患者相比,接受PLND治疗的患者无生化复发(BCR)生存率明显降低(P=0.019)。多变量分析显示,前列腺特异性抗原(PSA)水平高(p
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引用次数: 0
A Rare Subglottic Pleomorphic Adenoma: Magnetic Resonance Findings. 罕见的声门下多形性腺瘤:磁共振检查结果
IF 0.6 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2024-08-01 DOI: 10.18926/AMO/67549
Chieko Furukawa, Tomoyasu Tachibana, Tetsuji Nobuhisa, Yuichiro Kanie, Yoji Wani, Jun-Ya Matsumoto, Akifumi Kariya, Asuka Sato, Iichiro Ishikawa, Yuto Naoi, Mizuo Ando

No previous study has published magnetic resonance imaging (MRI) findings for a subglottic pleomorphic adenoma. Here, we describe the case of a 62-year-old man with a subglottic pleomorphic adenoma. Endoscopic findings revealed a smooth-surfaced tumor arising from the subglottic posterior wall. MRI revealed the lesion as an isointense region on T1-weighted images, which was homogeneously enhanced. This lesion showed a heterogeneously hyperintense region on T2-weighted images. Diffusion-weighted imaging (DWI) showed slightly high intensity in the same area, with a normal or only slightly high apparent diffusion coefficient (ADC). Laryngomicrosurgery was performed for transoral excision of the subglottic tumor, resulting in a postsurgical diagnosis of pleomorphic adenoma.

以前没有研究发表过声门下多形腺瘤的磁共振成像(MRI)结果。在此,我们描述了一名 62 岁男性声门下多形性腺瘤患者的病例。内窥镜检查结果显示,声门下后壁长了一个表面光滑的肿瘤。磁共振成像显示,病变在 T1 加权图像上为等密度区,呈均匀强化。该病灶在 T2 加权图像上显示为异质高密度区。弥散加权成像(DWI)显示同一区域的强度略高,表观弥散系数(ADC)正常或仅略高。患者接受了喉镜手术,经口切除了声门下肿瘤,术后诊断为多形性腺瘤。
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引用次数: 0
Pneumocephalus with Inverted Papilloma in the Frontoethmoidal Sinus: Case Report and Literature Review. 前牙状窦倒置乳头状瘤引发的气胸:病例报告和文献综述。
IF 0.6 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2024-08-01 DOI: 10.18926/AMO/67550
Seiichiro Makihara, Yoshihiro Otani, Kensuke Uraguchi, Sawako Ono, Aiko Shimizu, Ryosuke Ikemachi, Yosuke Okazaki, Tomoyuki Ota, Hiroshi Matsumoto, Shotaro Miyamoto, Munechika Tsumura, Seiya Hayashi, Michiari Umakoshi, Koji Hirashita, Mizuo Ando

Here, we describe the unique case of a pneumocephalus originating from an inverted papilloma (IP) in the frontoethmoidal sinus. A 71-year-old man with diabetes presented with headaches and altered consciousness. Imaging revealed the pneumocephalus together with bone destruction in the left frontal sinus. He underwent simultaneous endoscopic endonasal and transcranial surgery using an ORBEYE exoscope. Pathological diagnosis of the tumor confirmed IP. Post-surgery, the pneumocephalus was significantly resolved and the squamous cell carcinoma antigen level, which had been elevated, decreased. This case underscores the importance of a multidisciplinary approach and innovative surgical methods in treating complex sinonasal pathologies.

在这里,我们描述了一例独特的脑积气病例,该病源于前耳状窦的倒置乳头状瘤(IP)。一名 71 岁的男性糖尿病患者出现头痛和意识改变。影像学检查发现他患有脑积气,左侧额窦还伴有骨质破坏。他使用 ORBEYE 外窥镜同时接受了鼻内镜和经颅手术。肿瘤的病理诊断证实为 IP。手术后,气胸症状明显缓解,鳞状细胞癌抗原水平也有所下降。该病例强调了多学科方法和创新手术方法在治疗复杂鼻窦病变中的重要性。
{"title":"Pneumocephalus with Inverted Papilloma in the Frontoethmoidal Sinus: Case Report and Literature Review.","authors":"Seiichiro Makihara, Yoshihiro Otani, Kensuke Uraguchi, Sawako Ono, Aiko Shimizu, Ryosuke Ikemachi, Yosuke Okazaki, Tomoyuki Ota, Hiroshi Matsumoto, Shotaro Miyamoto, Munechika Tsumura, Seiya Hayashi, Michiari Umakoshi, Koji Hirashita, Mizuo Ando","doi":"10.18926/AMO/67550","DOIUrl":"https://doi.org/10.18926/AMO/67550","url":null,"abstract":"<p><p>Here, we describe the unique case of a pneumocephalus originating from an inverted papilloma (IP) in the frontoethmoidal sinus. A 71-year-old man with diabetes presented with headaches and altered consciousness. Imaging revealed the pneumocephalus together with bone destruction in the left frontal sinus. He underwent simultaneous endoscopic endonasal and transcranial surgery using an ORBEYE exoscope. Pathological diagnosis of the tumor confirmed IP. Post-surgery, the pneumocephalus was significantly resolved and the squamous cell carcinoma antigen level, which had been elevated, decreased. This case underscores the importance of a multidisciplinary approach and innovative surgical methods in treating complex sinonasal pathologies.</p>","PeriodicalId":7017,"journal":{"name":"Acta medica Okayama","volume":"78 4","pages":"337-343"},"PeriodicalIF":0.6,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142091403","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Acta medica Okayama
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